A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612799



Internal ID20985870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99922583..99936394hg38UCSC Ensembl
chr6:100370459..100384270hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3813812
hg1913812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147666
Samples
Known GenesMCHR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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